Canonical Allele Identifier: CA350793632

Gene: ABCA12 SNHG31

Linked Data

• MyVariant Identifiers: chr2:g.215809762C>A (hg19) ; chr2:g.214945038C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214945038C>A , CM000664.2:g.214945038C>A	GRCh38
NC_000002.11:g.215809762C>A , CM000664.1:g.215809762C>A	GRCh37
NC_000002.10:g.215518007C>A	NCBI36
NG_007074.1:g.198390G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272895.12:c.7306G>T (ABCA12) MANE Select	ENSP00000272895.7:p.Val2436Leu
ENST00000272895.11:c.7306G>T (ABCA12)	ENSP00000272895.7:p.Val2436Leu
ENST00000389661.4:c.6352G>T (ABCA12)	ENSP00000374312.4:p.Val2118Leu
NM_015657.3:c.6352G>T (ABCA12)	NP_056472.2:p.Val2118Leu
NM_173076.2:c.7306G>T (ABCA12)	NP_775099.2:p.Val2436Leu
NR_103740.1:n.7606G>T (ABCA12)
NR_110292.1:n.322-2787C>A (SNHG31)
XM_011510951.1:c.7315G>T (ABCA12)	XP_011509253.1:p.Val2439Leu
XM_011510951.2:c.7315G>T (ABCA12)	XP_011509253.1:p.Val2439Leu
NM_173076.3:c.7306G>T (ABCA12) MANE Select	NP_775099.2:p.Val2436Leu
NR_103740.2:n.7804G>T (ABCA12)
NM_015657.4:c.6352G>T (ABCA12)	NP_056472.2:p.Val2118Leu